US7108860B2 - Sunscreen compositions - Google Patents
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- US7108860B2 US7108860B2 US10448745 US44874503A US7108860B2 US 7108860 B2 US7108860 B2 US 7108860B2 US 10448745 US10448745 US 10448745 US 44874503 A US44874503 A US 44874503A US 7108860 B2 US7108860 B2 US 7108860B2
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILET PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K8/00—Cosmetics or similar toilet preparations
- A61K8/18—Cosmetics or similar toilet preparations characterised by the composition
- A61K8/72—Cosmetics or similar toilet preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K8/00—Cosmetics or similar toilet preparations
- A61K8/18—Cosmetics or similar toilet preparations characterised by the composition
- A61K8/72—Cosmetics or similar toilet preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toilet preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8147—Homopolymers or copolymers of acids; Metal or ammonium salts thereof, e.g. crotonic acid, (meth)acrylic acid; Compositions of derivatives of such polymers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K8/00—Cosmetics or similar toilet preparations
- A61K8/18—Cosmetics or similar toilet preparations characterised by the composition
- A61K8/72—Cosmetics or similar toilet preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toilet preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/51—Chelating agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/52—Stabilizers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/52—Stabilizers
- A61K2800/524—Preservatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL, OR TOILET PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/59—Mixtures
- A61K2800/594—Mixtures of polymers
Abstract
Description
This application claims priority from the U.S. provisional patent application bearing Application Ser. No. 60/386,317, filed on Jun. 6, 2002, now abandoned.
1. Field of the Invention
The present invention relates to cosmetic compositions that have enhanced rheological properties. More particularly, the present invention relates to sunscreen compositions that have enhanced rheological properties before and after application.
2. Description of the Prior Art
Cosmetic compositions, including sunscreens, are commercially available in various forms, such as lotions, creams, gels, and the like and are well known in the art. These compositions are typically formulated to have optimal rheological properties at or close to room temperature. One major drawback with these compositions is that they degrade rheologically at elevated temperatures, especially above room temperature. At these elevated temperatures, it has been found that the compositions no longer maintain the desired viscosity, resulting in a product that undesirably may drip or run during dispensing and/or application.
While all cosmetic compositions may be exposed to elevated temperatures, sunscreen compositions are especially susceptible to exposure to elevated temperatures due to the nature of their use. Sunscreen compositions are applied to the skin to protect the skin from the sun's ultraviolet rays that can lead to erythema, a reddening of the skin also known as sunburn. Sunlight or ultraviolet radiation in the UV-B range has a wavelength of 290 nm to 320 nm and is known to be the primary cause of sunburn. Ultraviolet rays at a wavelength of 320 nm to 400 nm, known as UV-A radiation, produces tanning of the skin. However, in the process of doing so, the UV-A rays can damage or harm the skin.
Besides the immediate malady of sunburn, excessive sunlight exposure can lead to skin disorders. For instance, prolonged and constant exposure to the sun may lead to actinic keratoses and carcinomas. Another long-term effect is premature aging of the skin. This condition is characterized by skin that is wrinkled, cracked and has lost its elasticity.
As stated above, sunscreens are typically formulated with the goal of inhibiting skin damage from the sun's rays. The sunscreen composition filters or blocks the harmful UV-A and UV-B rays that can damage and harm the skin. It is believed that sunscreen agents accomplish this by absorbing the UV-A and/or UV-B rays.
Consumers consider many factors when purchasing a sunscreen product, such as, the sun protection factor (SPF), how durable the product is after applying it over the skin, the shelf life of the product, and product form (i.e., lotions, gels, creams, and sprays). Another important and influential property of a sunscreen product considered by a consumer is how the product dispenses and how well the product spreads over the skin. Typically, consumers want a sunscreen that does not drip and/or run from the dispenser orifice, from the hand during application, or once applied to the skin. However, when exposed to the sun or elevated temperatures, typically sunscreen viscosities significantly decrease. This causes the sunscreen to drip and run from both the orifice of the dispenser and on the skin, making it very difficult for a user to evenly apply the sunscreen to the skin. In addition, the viscosity breakdown may result in a loss of product aesthetics, thus the product does not have a smooth, silky feel when applied to the skin, which is another important factor considered by consumers.
The cosmetic compositions of the present invention overcome the prior art deficiencies by providing a composition with a stable viscosity over a broad temperature range. As a result, the composition does not drip or run when dispensed and/or applied to the skin. In addition, the composition imparts an enhanced soft, silky feel when applied.
It is an object of the present invention to provide a cosmetic composition that can be effectively applied as a lotion, cream or gel.
It is another object of the present invention to provide such a cosmetic composition that has a stable viscosity over a broad range of temperatures.
It is still another object of the present invention to provide such a cosmetic composition that dispenses at elevated temperatures without dripping or running from the orifice of the dispenser.
It is a further object of the present invention to provide such a cosmetic composition that does not drip or run upon application to the skin at elevated temperatures.
It is still a further object of the present invention to provide such a cosmetic composition that has a soft, silky feel and spreads uniformly over the skin.
It is yet another object of the present invention to provide such a cosmetic composition that is a sunscreen composition.
It is still another object of the present invention to provide such a sunscreen composition that is a stable oil-in-water emulsion or gel.
To accomplish the foregoing objects and advantages, the present invention, in brief summary, is a cosmetic composition that has an amount of at least one rheology modifying agent, and more preferably at least two rheology modifying agents, such that the viscosity of the composition remains stable over a broad temperature range. The compositions of the present invention may also include at least one of the following additional components: sunscreen agent, SPF booster, secondary emulsifier, emollient, skin-feel additive, moisturizing agent, humectant, film former/waterproofing agent, bio-active (functional) ingredient, pH adjuster/chelating agent, preservative, fragrance, effect pigment, color additive, or any combinations thereof.
The compositions of the present invention are uniquely formulated to provide not only a stable viscosity over a broad temperature range, but an enhanced feeling of softness and silkiness when the sunscreen composition is applied to the skin. Moreover, the compositions are capable of easy and uniform application over the skin. These enhanced properties are achieved, in large part, by formulating the compositions with an at least one rheology modifying agent, and more preferably two or more rheology modifying agents such that the viscosity remains stable over a broad temperature range.
In addition, the cosmetic compositions may include one or more of the following components: sunscreen agent, SPF booster, secondary emulsifier, emollient, moisturizer, humectant, film former/waterproofing agent, bio-active (functional) ingredient, pH adjuster/chelating agent, preservative, fragrance, effect pigment, color additive or any combinations thereof.
It has been unexpectedly found that the inclusion of two or more rheology modifying agents according to the present invention provides a synergistic effect that results in compositions having a stable viscosity over a broad temperature range. By way of example, the compositions of the present invention unexpectedly exhibit a stable viscosity over a temperature range of about 20° C. to about 70° C.
The term “stable viscosity”, as used herein is meant to define a composition having a viscosity that does not deviate more than about 20% from an initially measured viscosity. Preferably, the stable viscosity does not deviate more than 10% from an initially measured viscosity. More preferably, the viscosity does not deviate more than 5% from an initially measured viscosity of a composition of the present invention.
Suitable rheology modifying agents for use in the compositions of the present invention include, but are not limited to, one or more polymeric emulsifiers, thickening agents, synthetic and natural gum or polymer products, polysaccharide thickening agents, stabilizers, associative thickeners, anionic associative rheology modifiers, nonionic associative rheology modifiers, oil-thickening agents, or any combinations thereof. Preferably, the rheology modifying agents are one or more polymeric emulsifiers in combination with one or more thickening agents.
Suitable polymeric emulsifiers for use in the compositions of the present invention include, but are not limited to, acrylates crosspolymer, acrylates/C10-30 alkylacrylate crosspolymer, acrylates/vinyl isodecanoate crosspolymer, polyacrylic acid, sodium polymethacrylate, sodium polyacrylate, polyacrylates, or any combinations thereof. Preferably, the polymeric emulsifier is acrylates/C10-30 alkylacrylate crosspolymer, acrylates/vinyl isodecanoate crosspolymer, or a combination thereof. The polymeric emulsifiers used as rheological modifying agents assist in building a matrix in the composition.
The amount of emulsifier present in the compositions of the present invention is about 0.01 weight percent (wt. %) to about 10 wt. % of the total weight of the composition. Preferably, the emulsifier is present in an amount about 0.1 wt. % to about 5 wt. % of the total weight of the composition.
Suitable thickening agents that may be used as rheological modifying agents in the compositions of the present invention include, but are not limited to, one or more stabilizers, synthetic and natural gum or polymer products, polysaccharide thickening agents, associative thickeners, anionic associative rheology modifiers, nonionic associative rheology modifiers, oil-thickening agents, acrylates/C10–30 alkylacrylate crosspolymer, acrylates/aminoacrylates/C10–30 alkyl PEG-20 itaconate copolymer, acrylates copolymer, acrylates/steareth-20 methacrylate copolymer, acrylates/beheneth-25 methacrylate copolymer, PEG-150/decyl alcohol/SMDI copolymer, PVP, PVM/MA decadiene crosspolymer, carbomer, PEG crosspolymer, acrylates/palmeth-25 acrylates copolymer, polysaccharides, polyacrylates, polyether-1, sodium magnesium silicates, sodium carbomers, sodium polyacrylates, sodium polymethacrylates, sodium polyacryloyldimethyl taurates, sodium acryloyldimethyl taurate copolymers, sodium carragenan, sodium carboxymethyl dextran, hydroxyethylcellulose, hydroxypropyl cyclodextran, bentonites, trihydroxystearin, aluminum-magnesium hydroxide stearate, xanthan gum, or any combinations thereof. Preferably, the thickening agent is carbomer, sodium carbomer, xanthan gum, or any combinations thereof.
The amount of thickening agent present in the compositions of the present invention is about 0.01 wt. % to about 10 wt. % of the total weight of the composition. Preferably, the thickener is present in an amount about 0.1 wt. % to about 5 wt. % of the total weight of the composition.
It has been unexpectedly found that by including a combination of one or more emulsifiers with one or more thickening agents in a concentration ratio of about 1:10 to about 10:1, preferably about 1:5 to about 5:1, and more preferably about 1:2 to about 2:1, respectively, results in compositions having a stable viscosity over a broad temperature range.
When it is desired to formulate a sunscreen composition, one or more sunscreen agents may be included in the compositions of the present invention. The one or more sunscreen agents that can be used in the present invention must be capable of absorbing or blocking the harmful effects of ultraviolet radiation. In addition, they must be non-toxic and non-irritating when applied to the skin. Suitable sunscreen agents that may be used in the sunscreen composition include, but are not limited to, para-aminobenzoic acid (PABA), butyl methoxydibenzoylmethane (avobenzone), benzophenone-1, benzophenone-2, benzophenone-3, benzophenone-4, benzophenone-6, benzophenone-8, benzophenone-12, bis-ethylhexyloxyphenol methoxyphenyl triazine, methoxycinnamate, ethyl dihydroxypropyl-PABA, glyceryl PABA, homosalate, methyl anthranilate, octocrylene, octyl dimethyl PABA, octyl methoxycinnamate, octyl salicylate, PABA, 2-phenylbenzimidazole-5-sulphonic acid, triethanolamine salicylate, 3-(4-methylbenzylidene)-camphor, red petrolatum, zinc oxide, titanium dioxide, 3-(4-methylbenzyldine)boran-2-one(methylbenzindinecamphor), benzotriazole, octyl triazone, phenylbenzimidazole-5-sulfonic acid, methylene bis-benzotrizolyl tetramethylbutyl phenol, or any combinations thereof.
The one or more sunscreen agents are included in the present composition at about 1 wt. % to about 40 wt. % of the total weight of the composition. The amount of sunscreen agent in the composition will vary in the above range depending on the sun protection factor (SPF) desired. The higher the SPF, the greater the total amount of sunscreen agent. Preferably, the one or more sunscreen agents are included at about 2 wt. % to about 35 wt. % to achieve a SPF of about 2 to about 50. More preferably, the one or more sunscreen agents are included in an amount about 4 wt. % to about 20 wt. % to achieve a SPF value of about 4 to about 30.
The compositions of the present invention also include one or more diluents. Suitable diluents include, but are not limited to, water, glycol or any combinations thereof. Preferably, the diluent is water. The diluent is present in the compositions of the present invention in an amount about 40 wt. % to about 90 wt. %, and preferably about 50 wt. % to about 80 wt. %, of the total weight of the compositions.
In addition to the one or more polymeric emulsifiers, which are primary emulsifiers, one or more secondary emulsifiers may be included in the compositions of the present invention. The one or more secondary emulsifiers are not matrix building emulsifiers, like the primary, polymeric emulsifiers used as the rheological modifying agent. The secondary emulsifier actually reduces particle size in the emulsion of the composition. The one or more secondary emulsifiers suitable for use in the present invention include, but are not limited to, cetyl alcohol, cetearyl alcohol, oleth-10, diethylhexyl esters, sorbitan oleate, sorbitan sesquioleate, sorbitan isostearate, sorbitan trioleate, PEG-20 almond glycerides, polyglyceryl-3-diisostearate, polyglycerol esters of oleic/isostearic acid, polyglyceryl-6 hexaricinolate, polyglyceryl-4-oleate, polygylceryl-4 oleate/PEG-8 propylene glycol cocoate, sodium glyceryl oleate phosphate, hydrogenated vegetable glycerides phosphate, or any combinations thereof.
The amount of secondary emulsifier present in the compositions of the present invention is about 0.01 wt. % to about 5 wt. % of the total weight of the composition. Preferably, one or more additional emulsifiers are present in an amount about 0.05 wt. % to about 2 wt. % and more preferably in an amount about 0.1 wt. % to about 0.5 wt. %, based on the total weight of the composition.
The present compositions may include one or more emollients. An emollient provides a softening, protective or soothing effect on the skin surface and is generally considered safe for topical use. It also helps control the rate of evaporation and the tackiness of the compositions.
A suitable emollient for use in the present compositions include, but is not limited to, cocoglycerides, cyclomethicone, dimethicone, dicapryl maleate, caprylic/capric triglyceride, isopropyl myristate, octyl stearate, isostearyl linoleate, lanolin oil, coconut oil, cocoa butter, olive oil, avocado oil, aloe extracts, jojoba oil, castor oil, fatty acid such as oleic and stearic, fatty alcohol such as cetyl and hexadecyl, diisopropyl adipate, hydroxybenzoate ester, benzoic acid esters of C9–C15 alcohols, isononyl iso-nonanoate, alkane such as mineral oil, silicone such as dimethyl polysiloxane, ether such as polyoxypropylene butyl ether and polyoxypropylene cetyl ether, C12–C15 alkyl benzoate, or any combinations thereof.
The total amount of emollient present in the compositions is typically about 0.1 wt. % to about 30 wt. % of the total weight of the composition. Preferably, emollient is present in an amount about 1 wt. % to about 20 wt. % of the total weight of the composition.
The pH of the compositions of the present invention may be adjusted by one or more pH adjusters and/or chelating agents. For example, sodium hydroxide, triethanolamine, EDTA salt, or any combinations thereof, are suitable pH adjusters/chelating agents that may be included in the sunscreen compositions of the present invention.
An effective amount of a pH adjuster and/or chelating agent is included to adjust the pH of the final composition to about 3 to about 9. Preferably, the pH is adjusted to about 5 to about 8 and more preferably about 6 to about 7.
One or more humectants may be used in the compositions of the present invention. Suitable humectants include, but are not limited to, glycerin, pentylene glycol, hexylene glycol, propylene glycol, butylene glycol, sorbitol, PEG-4, or any combinations thereof.
One or more humectants may be included in the compositions of the present invention in an amount about 0.1 wt. % to about 15 wt. % of the total weight of the composition. Preferably, humectant is present in an amount about 1 wt. % to about 5 wt. % of the total weight of the composition.
The present compositions may include one or more SPF boosters. The SPF booster itself is not an active ingredient, but is designed to enhance the effectiveness of the sunscreen actives present in the formulation. Suitable SPF boosters include, but are not limited to, styrene/acrylates copolymer, sodium bentonite, highly purified white sodium bentonite, montmorillonite, hydrogel, or any combinations thereof. A preferred styrene/acrylates copolymer for use in the present invention is sold under the trade name SunSpheres® by Rohm and Haas Company.
When present, the one or more SPF boosters may be included in the compositions of the present invention in an amount about 1 wt. % to about 6 wt. % of the total weight of the composition. Preferably, SPF booster is present in an amount about 2 wt. % to about 3 wt. % of the total weight of the composition.
Another component that may be used in the compositions of the present invention is a film former/waterproofing agent. The film former/waterproofing agent is a hydrophobic material that imparts film forming and waterproofing characteristics to the emulsion. Suitable film former/waterproofing agent for use in the compositions of the present invention include, but is not limited to, acrylates/acrylamide copolymer, acrylates copolymer, acrylates/C12-22 alkylmethacrylate copolymer, polyethylene, waxes, VP/dimethiconylacrylate/polycarbamylpolyglycol ester, butylated PVP, PVP/hexadecene copolymer, octadecene/MA copolymer, PVP/eicosene copolymer, tricontanyl PVP, Brassica Campestris/Aleuritis Fordi Oil copolymer, decamethyl cyclopentasiloxane (and) trimethylsiloxysilicate, or any combinations thereof.
In a preferred embodiment, the film former/waterproofing agent is acrylates/C12-22 alkylmethacrylate copolymer sold under the tradename Allianz OPT® by ISP.
One or more film formers/waterproofing agents may be present in the compositions of the present invention in an amount about 0.1 wt. % to about 5 wt. % of the total weight of the composition. Preferably, the one or more film formers/waterproofing agents is present in the compositions of the present invention in an amount about 1 wt. % to about 3 wt. % of the total weight of the composition.
In addition, it has been unexpectedly found that the acrylates/C12-22 alkylmethacrylate copolymer may protect the lipids in a user's skin by imparting structure to the epidermal lipids in the skin (stratum corneum) and sebaceous lipids (sebum) and preventing them from depletion. As a result, it is believed that the acrylates/C12-22 alkylmethacrylate copolymer may enhance and help to maintain the barrier properties of the lipid barrier in stratum corneum.
Therefore, the compositions of the present invention may exhibit moisturizing and anti-inflammatory properties without a need for including moisturizers and/or anti-inflammatory agents in the compositions.
One or more preservatives may be included in the compositions of the present invention. The preservative protects the compositions from microbial contamination and/or oxidation. As such, the preservative can include an antioxidant. Preservatives, such as diazolidinyl urea, iodopropynyl butylcarbamate, chloromethylisotiazolinone, methylisothiazolinone, vitamin E and its derivatives including vitamin E acetate, vitamin C, butylated hydroxytoluene, butylparaben, ethylparaben, methylparaben, propylparaben, isobutylparaben, phenoxyethanol, or any combinations thereof, may be included as a preservative in a composition of the present invention.
Preferably, in one embodiment of the present invention, the preservative is a combination of phenoxyethanol, methylparaben, ethylparaben, propylparaben, isobutylparaben and butylparaben sold under the tradename Phenonip® by Nipa.
About 0.01 wt. % to about 2 wt. % of preservative may be included in a composition of the present invention. Preferably, one or more preservatives total about 0.5 wt. % to about 1.5 wt. % of the total weight of the composition.
The compositions of the present invention may also have other optional additives including bio-active (functional) ingredients. For instance, one or more plant extracts, fruit extracts, vegetable extracts, algae extracts, sugars, polysaccharides, lipids, proteins, peptides, aminoacids, aminoacid derivatives, absorbents, salicylic acid, alpha and beta hydroxy acids, oil and water soluble vitamins including vitamins A, C, and E and their derivatives, or any combinations thereof, may be included in the sunscreen compositions.
When present, the optional additives may be included in the present composition in an amount about 0.001 wt. % to about 10 wt. %, based on the total weight of the composition.
In one embodiment of the present invention, the components of the present invention may be combined to form stable oil-in-water emulsion sunscreen compositions. The one or more sunscreen agents are preferably incorporated into the oil phase and later combined with water with the help of the one or more emulsifiers. The process used to manufacture the composition of the present invention must be capable of forming a homogeneous composition that can be spread into a film.
In one preferred embodiment of the present invention, a sunscreen composition is formulated with about 2 wt. % to about 12 wt. % of sunscreen agent including octinoxate, octocrylene, or any combination thereof; and a combination of carbomer and acrylates/C10-30 alkyl acrylate crosspolymer present in an amount about 0.1 wt. % to about 0.5 wt. % and a ratio of about 1:2 to about 2:1. This composition has been found to have a stable viscosity over a broad temperature range. It has also been found to have an enhanced soft, silky feel when applied to the skin. In addition, this composition has a SPF of at least 15. In a more preferred embodiment, this composition also includes about 1 wt. % to about 2 wt. % of acrylates/C12-22 alkylmethacrylate copolymer, which imparts a waterproof property to the composition and unexpectedly imparts moisturizing properties to a user's skin.
In a second preferred embodiment of the present invention, a sunscreen composition is formulated with about 1 wt. % to about 8 wt. % of sunscreen agent including octinoxate, octisalate, or any combination thereof; and about 0.1 wt. % to about 0.5 wt. % of a combination of carbomer and acrylates/C10-30 alkyl acrylate crosspolymer present in a ratio of about 1:2 to about 2:1. This composition has been found to have a stable viscosity over a broad temperature range. It has also been found to have an enhanced soft, silky feel when applied to the skin. In addition, this composition has a SPF of at least 8. In a more preferred embodiment, this composition also includes about 1 wt. % to about 2 wt. % of acrylates/C12-22 alkylmethacrylate copolymer, which imparts a waterproof property to the composition and unexpectedly imparts moisturizing properties to a user's skin.
In a third preferred embodiment of the present invention, a sunscreen composition is formulated with about 1 wt. % to about 4 wt. % of sunscreen agent; and about 0.1 wt. % to about 0.5 wt. % of a combination of carbomer and acrylates/C10-30 alkylacrylate crosspolymer present in a ratio of about 1:2 to about 2:1. The sunscreen agent includes octinoxate, octisalate, or any combination thereof. This composition has been found to have a stable viscosity over a broad temperature range. It has also been found to have an enhanced soft, silky feel when applied to the skin. In addition, this composition has a SPF of at least 4. In a more preferred embodiment, this composition also includes about 1 wt. % to about 2 wt. % of acrylates/C12-22 alkylmethacrylate copolymer, which imparts a waterproof property to the composition and unexpectedly imparts moisturizing properties to a user's skin.
In a fourth preferred embodiment of the present invention, a sunscreen composition is formulated with about 1.5 wt. % to about 20 wt. % of one or more sunscreen agents; and a combination of carbomer, xanthan gum and acrylates/C10-30 alkyl acrylate crosspolymer present in an amount about 0.1 wt. % to about 0.5 wt. % and a ratio of about 1:2 to about 2:1. The sunscreen agent includes avobenzone, octinoxate, octisalate, oxybenzone, or any combinations thereof. This composition has been found to have a stable viscosity over a broad temperature range. It has also been found to have an enhanced soft, silky feel when applied to the skin. In addition, this composition has a SPF of at least 30.
Product A contains the following active ingredients: homosalate, octyl methoxycinnamate, octyl salicylate, and oxybenzone and the following inactive ingredients: water, PEG-8, silica dimethyl silylate, cetyl phosphate, acrylates/C10–30 alkyl acrylate crosspolymer, tocopherol (Vitamin E), propylene glycol, methylparaben, propylparaben, disodium EDTA, diazolidinyl urea, triethanolamine, and fragrance.
Product B contains the following active ingredients: homosalate, octyl methoxycinnamate, octyl salicylate, oxybenzone, and avobenzone and the following inactive ingredients: water, PEG-8, benzyl alcohol, cetyl phosphate, acrylates/C10–30 alkyl acrylate crosspolymer, propylene glycol, methylparaben, propylparaben, disodium EDTA, triethanolamine, and silica dimethyl silylate.
Product C contains the following active ingredients: homosalate, octyl methoxycinnamate, octyl salicylate, and oxybenzone, and the following inactive ingredients: water, PEG-8, silica dimethyl silylate, cetyl phosphate, acrylates/C10–30 alkyl acrylate crosspolymer, tocopherol (Vitamin E), propylene glycol, methylparaben, propylparaben, disodium EDTA, diazolidinyl urea, triethanolamine, carbomer, and fragrance.
Product D contains the following active ingredients: octyl methoxycinnamate, octyl salicylate, and oxybenzone, and the following inactive ingredients: water, ethylhexyl palmitate, PEG-8, silica dimethyl silylate, cetyl phosphate, acrylates/C10–30 alkyl acrylate crosspolymer, tocopherol (Vitamin E), propylene glycol, methylparaben, propylparaben, disodium EDTA, diazolidinyl urea, triethanolamine, carbomer, and fragrance.
Product E contains the following active ingredients: octyl methoxycinnamate, octyl salicylate, oxybenzone, and homosalate, and the following inactive ingredients: water, sorbitan isostearate, sorbitol, polyglyceryl-3 distearate, octadecene/MA copolymer, triethanolamine, stearic acid, barium sulfate, benzyl alcohol, dimethicone, aloe barbadensis extract, jojoba oil, tocopherol (Vitamin E), methylparaben, propylparaben, disodium EDTA, diazolidinyl urea, carbomer, and fragrance.
Table 1 below indicates Brookfield viscosity changes of a sunscreen composition according to the present invention as compared to four competitor sunscreen products, namely Products A, B, C and D.
TABLE 1
Brookfield Viscosities
Brookfield Viscosity cps, TB/5 rpm/1 min/Average
of 6 measurements/with Helipath/at:
SAMPLE
22.5 C (Room t° )
45° C.
45° C., %
55° C.
55° C., %
65° C.
65° C., %
Sunscreen
27,200 (100%)
27,500
1.10%
25,800
−5.10%
25,700
−5.50%
Composition of
Present
Invention
Product A
25,550 (100%)
15,500
−39.30%
15,000
−41%
11,780
−53.40%
Product B
17,500 (100%)
11,700
−33.10%
12,050
−31.14%
10,900
−37.70%
Product C
24,200 (100%)
16,000
−33.90%
15,900
−34.30%
13,600
−43.80%
Product D
24,250 (100%)
17,100
−29.40%
17,000
−29.90%
14,500
−40.20%
As is evident from the data set forth above, the composition of the present invention only deviates at most about 5.5% from its original viscosity at room temperature, over a broad temperature range increase, as opposed to the far greater deviation experienced by the competitor products. This critical property of the present invention is also illustrated in
The compositions of the present invention may be prepared according to techniques and methods well known in the art. By way of example, ingredients are incorporated by mixing and applying heat if necessary, until the composition is uniform and homogeneous. The composition may be homogenized to ensure homogeneity and to build the proper viscosity. The sunscreen compositions of the present invention are then packaged as a lotion in any package or container suitable for a sunscreen composition.
Having thus described the present invention with particular reference to preferred embodiments thereof, it will be apparent that various changes and modifications may be made therein without departing from the spirit and scope of the present invention.
Claims (79)
Priority Applications (2)
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US38631702 true | 2002-06-06 | 2002-06-06 | |
US10448745 US7108860B2 (en) | 2002-06-06 | 2003-05-29 | Sunscreen compositions |
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US10448745 US7108860B2 (en) | 2002-06-06 | 2003-05-29 | Sunscreen compositions |
CA 2488335 CA2488335C (en) | 2002-06-06 | 2003-06-04 | Sunscreen compositions |
PCT/US2003/017570 WO2003103615A1 (en) | 2002-06-06 | 2003-06-04 | Sunscreen compositions |
GB0500022A GB2407268B (en) | 2002-06-06 | 2003-06-04 | Sunscreen compositions |
Publications (2)
Publication Number | Publication Date |
---|---|
US20040028709A1 true US20040028709A1 (en) | 2004-02-12 |
US7108860B2 true US7108860B2 (en) | 2006-09-19 |
Family
ID=29739901
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US10448745 Active 2024-10-19 US7108860B2 (en) | 2002-06-06 | 2003-05-29 | Sunscreen compositions |
Country Status (4)
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US (1) | US7108860B2 (en) |
CA (1) | CA2488335C (en) |
GB (1) | GB2407268B (en) |
WO (1) | WO2003103615A1 (en) |
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Citations (73)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3003063A (en) | 1959-03-12 | 1961-10-03 | Messen Jaschin G A | Apparatus for measuring radioactivity |
US4481186A (en) | 1983-05-27 | 1984-11-06 | Charles Of The Ritz Group Ltd. | Non-irritating cosmetic composition containing glucamine fatty acid emulsifier soap |
US4806344A (en) | 1987-01-05 | 1989-02-21 | Gaskin Frances C | Sun protectant composition and method |
US4933177A (en) | 1981-02-27 | 1990-06-12 | Societe Anonyme Dite: L'oreal | Cosmetic compositions for the treatment of the hair and skin contain in the form of a powder particles resulting from the pulverization of at least one plant substance and a cohesion agent |
US4954332A (en) | 1987-10-22 | 1990-09-04 | The Procter & Gamble Company | Photoprotection compositions comprising tocopherol sorbate and an anti-inflammatory agent |
US5116604A (en) | 1991-01-16 | 1992-05-26 | Bernel Chemical Co. | Sunscreen compositions containing novel neopentanoate esters |
US5208013A (en) | 1991-06-03 | 1993-05-04 | Olympus International, Inc. | Composition for skin care and protection |
US5306485A (en) | 1991-05-07 | 1994-04-26 | Richardson-Vicks Inc. | Suncare compositions |
US5445815A (en) | 1993-11-22 | 1995-08-29 | Siegfried; Robert W. | Dry sunscreen composition |
US5543136A (en) | 1994-06-16 | 1996-08-06 | Nuskin International, Inc. | Sunscreen emulsions |
US5547659A (en) | 1991-05-07 | 1996-08-20 | Richardson-Vicks Inc. | Photoprotection compositions |
US5560917A (en) | 1995-02-01 | 1996-10-01 | Maybelline Intermediate Company | Cosmetic makeup composition |
US5587150A (en) | 1990-02-14 | 1996-12-24 | L'oreal | Photostable cosmetic screening composition containing a UV-A screening agent and an alkyl β, β-diphenylacrylate or α-cyano-β,β-diphenylacrylate |
US5667765A (en) | 1994-06-03 | 1997-09-16 | L'oreal | Photoprotective/cosmetic compositions comprising at least one solid organic sunscreen compound and salicylate solvents therefor |
US5672337A (en) | 1994-12-12 | 1997-09-30 | L'oreal | Amido photostabilization of dibenzoylmethane sunscreens |
US5676934A (en) | 1993-11-22 | 1997-10-14 | International Creations, Ltd. | Dry sunscreen composition |
US5725844A (en) | 1993-02-11 | 1998-03-10 | Beiersdorf Ag | Waterproof cosmetic or dermatological photoprotective preparations |
US5770183A (en) | 1996-08-01 | 1998-06-23 | Linares; Francisco J. | High SPF (30 and over) waterproof sunblock compositions |
EP0848944A2 (en) | 1996-11-21 | 1998-06-24 | The C.P. Hall Company | Sunscreen composition comprising long, branched chain alkyl benzoates or hydroxybenzoates |
US5824323A (en) | 1996-11-01 | 1998-10-20 | Absolute Beauty Company | Skin lotion composition and softgel filled therewith and methods for making and using same |
US5863546A (en) | 1997-03-02 | 1999-01-26 | Swinehart; James M | Cosmetic composition |
EP0930063A2 (en) | 1997-12-04 | 1999-07-21 | The C.P. Hall Company | Skin care and sunscreen composition |
US5961961A (en) | 1998-06-04 | 1999-10-05 | Chesebrough-Pond's Usa Co. | Sunscreen cosmetic composition |
US5976560A (en) | 1998-01-30 | 1999-11-02 | Han; Nam Fong | Vegetable derived petroleum jelly replacement |
US5985251A (en) | 1997-12-01 | 1999-11-16 | Roche Vitamins Inc. | Light screening compositions |
US5989529A (en) | 1998-11-20 | 1999-11-23 | Schering-Plough Healthcare Products, Inc. | Substantive topical composition |
US6007846A (en) | 1997-05-16 | 1999-12-28 | Townley Jewelry, Inc. | Scented body gel having particulate matter in the form of glitter with predetermined shapes |
US6043204A (en) | 1997-11-07 | 2000-03-28 | Kaufman; Stacy R. | Body cleansing composition providing protection against sunburn after rinsing |
US6048517A (en) | 1996-11-25 | 2000-04-11 | Schering-Plough Healthcare Products, Inc. | High SPF sunscreen formulations |
US6071501A (en) | 1999-02-05 | 2000-06-06 | The Procter & Gamble Company | Photostable UV protection compositions |
US6090369A (en) | 1997-06-04 | 2000-07-18 | Stewart; Ernest Glading | Sunscreen formulation with avobenzone and method for stabilizing sunscreen formulation which contains avobenzone |
WO2000057850A1 (en) | 1999-03-25 | 2000-10-05 | Haarmann & Reimer | Photostable sunscreen compositions containing dibenzoylmethane derivative, e.g., parsol® 1789, and diesters or polyesters of naphthalene dicarboxylic acid photostabilizers and enhancers of the sun protection factor (spf) |
US6153208A (en) | 1997-09-12 | 2000-11-28 | The Procter & Gamble Company | Cleansing and conditioning article for skin or hair |
US6159453A (en) | 1997-01-16 | 2000-12-12 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Sunscreens for protection from sun radiation |
US6162448A (en) | 1997-05-28 | 2000-12-19 | L'oreal | Combination of a retinoid with a polyamine polymer |
US6165451A (en) | 1999-02-08 | 2000-12-26 | Roche Vitamins Inc. | Cosmetic light screening composition |
US6190645B1 (en) | 1999-07-15 | 2001-02-20 | Playtex Products, Inc. | Sunscreen for the scalp hair and hair |
US6197281B1 (en) | 1997-06-04 | 2001-03-06 | Ernest G. Stewart | Wet appliable, instant protection sunscreen and makeup and method of use |
US6210658B1 (en) | 2000-06-12 | 2001-04-03 | The C. P. Hall Corporation | Stable sunscreen composition containing a barium compound, e.g., barium sulfate, a dibenzoylmethane derivative, e.g., butyl methoxydibenzoylmethane (avobenzone), and a methoxycinnamate derivative, e.g., octyl methoxycinnamate |
US6224852B1 (en) | 1999-04-23 | 2001-05-01 | Unilever Home & Personal Care Usa | Liquid sunscreen compositions which both deposit and lather well |
US6238650B1 (en) | 1999-05-26 | 2001-05-29 | Sol-Gel Technologies Ltd. | Sunscreen composition containing sol-gel microcapsules |
US20010014314A1 (en) | 1999-02-11 | 2001-08-16 | Marie Harbeck | Foot soap composition |
US6290938B1 (en) | 1998-07-30 | 2001-09-18 | The Procter & Gamble Company | Sunscreen compositions |
US20010026789A1 (en) | 1998-07-10 | 2001-10-04 | Herve Richard | Photostabilized sunscreen compositions comprising dibenzoylmethane compounds and benzylidenecamphor-substituted silanes/organosiloxanes |
US20010031247A1 (en) | 2000-02-08 | 2001-10-18 | Martin Josso | UV-photoprotecting sunscreen compositions comprising immixture of polyethylene/carboxylated polyethylene polymers |
US6322776B1 (en) | 1999-06-18 | 2001-11-27 | Schering-Plough Healthcare Products, Inc. | Anhydrous high-SPF ultraviolet light screens |
US6338838B1 (en) | 1999-05-12 | 2002-01-15 | Roche Vitamins Inc. | Photostable cosmetic light screening compositions |
US6342208B1 (en) | 1996-08-02 | 2002-01-29 | Plum Kerni Produktion A/S | Oil-in-water emulsion containing C10-C24 fatty acid derivatives for treating skin of mammals |
US20020012640A1 (en) | 2000-06-13 | 2002-01-31 | Fatemeh Mohammadi | Cosmetic composition for stressed skin under extreme conditions |
US6352685B2 (en) | 1999-12-24 | 2002-03-05 | KOSé CORPORATION | External preparation for skin |
US20020028875A1 (en) | 2000-07-20 | 2002-03-07 | Anderle Gary A. | Plasticized waterborne polyurethane dispersions and manufacturing process |
US20020028185A1 (en) | 2000-07-06 | 2002-03-07 | Fisher Gary J. | UVA (> 360-400) and UVB (300-325) specific sunscreens |
US6355264B1 (en) | 1998-03-20 | 2002-03-12 | Avon Products, Inc. | Insect repellent composition |
US20020037261A1 (en) | 1998-12-18 | 2002-03-28 | Nao Lapidot | Sunscreen composition containing sol-gel microcapsules |
US6365630B1 (en) | 1997-06-04 | 2002-04-02 | Regents Of The University Of Michigan | Compositions and methods for inhibiting photoaging of skin |
US6368639B1 (en) | 2000-03-24 | 2002-04-09 | Council Of Scientific And Industrial Research | Herbal skin care formulation and a process for the preparation thereof |
US6372234B1 (en) | 1997-05-27 | 2002-04-16 | Sembiosys Genetics Inc. | Products for topical applications comprising oil bodies |
US6384023B2 (en) | 1999-05-28 | 2002-05-07 | Neutrogena Corporation | Silicone gel containing salicylic acid |
US6395269B1 (en) | 1999-08-16 | 2002-05-28 | Playtex Products, Inc. | Sunscreen lotion or spray composition |
US6416748B1 (en) | 1999-10-22 | 2002-07-09 | Societe L'oreal | Emulsifier-free UV-photoprotecting emulsions comprising micronized insoluble screening agents |
US20020106337A1 (en) | 1997-05-27 | 2002-08-08 | Deckers Harm M. | Products for topical applications comprising oil bodies |
US6433061B1 (en) | 2000-10-24 | 2002-08-13 | Noveon Ip Holdings Corp. | Rheology modifying copolymer composition |
US6432389B1 (en) | 2001-07-06 | 2002-08-13 | Societe L'oreal | High SPF nontacky/nongreasy UV-photoprotecting compositions comprising particulates of MMA crosspolymers |
US6436376B1 (en) | 2001-02-26 | 2002-08-20 | Societe L'oreal S.A. | Enhanced SPF UV-sunscreen/tricontanyl PVP photoprotecting (sprayable) formulations |
US6436374B1 (en) | 1997-11-12 | 2002-08-20 | Merck Patent Gesellschaft Mit Beschraenkter Haftung | Light-stable cosmetic formulation containing butylmethoxydibenzoylmethane |
US6436377B1 (en) | 2001-02-26 | 2002-08-20 | Societe L'oreal S.A. | Enhanced SPF sunscreen (sprayable) formulations comprising interpolymers of PVP/dimethiconylacrylate/polycarbamyl/polyglycol ester |
US6458372B1 (en) | 2000-03-08 | 2002-10-01 | Color Access, Inc. | Gel powder composition |
US6458888B1 (en) | 2000-09-15 | 2002-10-01 | Isp Investments Inc. | Rheology modifier for use in aqueous compositions |
US6485712B1 (en) | 2001-05-24 | 2002-11-26 | Won Kyu Kim | UV blocking and slimming cosmetic composition |
US6488915B1 (en) | 2001-03-15 | 2002-12-03 | Basf Aktiengesellschaft | Use of sunscreen combinations which comprise, as essential constituent, 2-(4-alkoxyanilinomethylene) malonic dialkyl esters as photostable UV filters in cosmetic and pharmaceutical preparations |
US6495122B2 (en) | 1999-07-12 | 2002-12-17 | Ciba Specialty Chemicals Corporation | Use of mixtures of micropigments for preventing tanning and for lightening skin and hair |
US20020197217A1 (en) | 2001-06-06 | 2002-12-26 | Sewon Kang | Method and device for human skin tanning with reduced skin damage |
US6521217B1 (en) | 1998-06-22 | 2003-02-18 | Ciba Specialty Chemicals Corporation | Sun screen formulations |
Patent Citations (75)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3003063A (en) | 1959-03-12 | 1961-10-03 | Messen Jaschin G A | Apparatus for measuring radioactivity |
US4933177A (en) | 1981-02-27 | 1990-06-12 | Societe Anonyme Dite: L'oreal | Cosmetic compositions for the treatment of the hair and skin contain in the form of a powder particles resulting from the pulverization of at least one plant substance and a cohesion agent |
US4481186A (en) | 1983-05-27 | 1984-11-06 | Charles Of The Ritz Group Ltd. | Non-irritating cosmetic composition containing glucamine fatty acid emulsifier soap |
US4806344A (en) | 1987-01-05 | 1989-02-21 | Gaskin Frances C | Sun protectant composition and method |
US4954332A (en) | 1987-10-22 | 1990-09-04 | The Procter & Gamble Company | Photoprotection compositions comprising tocopherol sorbate and an anti-inflammatory agent |
US5587150A (en) | 1990-02-14 | 1996-12-24 | L'oreal | Photostable cosmetic screening composition containing a UV-A screening agent and an alkyl β, β-diphenylacrylate or α-cyano-β,β-diphenylacrylate |
US5116604A (en) | 1991-01-16 | 1992-05-26 | Bernel Chemical Co. | Sunscreen compositions containing novel neopentanoate esters |
US5306485A (en) | 1991-05-07 | 1994-04-26 | Richardson-Vicks Inc. | Suncare compositions |
US5547659A (en) | 1991-05-07 | 1996-08-20 | Richardson-Vicks Inc. | Photoprotection compositions |
US5208013A (en) | 1991-06-03 | 1993-05-04 | Olympus International, Inc. | Composition for skin care and protection |
US5725844A (en) | 1993-02-11 | 1998-03-10 | Beiersdorf Ag | Waterproof cosmetic or dermatological photoprotective preparations |
US5445815A (en) | 1993-11-22 | 1995-08-29 | Siegfried; Robert W. | Dry sunscreen composition |
US5676934A (en) | 1993-11-22 | 1997-10-14 | International Creations, Ltd. | Dry sunscreen composition |
US5667765A (en) | 1994-06-03 | 1997-09-16 | L'oreal | Photoprotective/cosmetic compositions comprising at least one solid organic sunscreen compound and salicylate solvents therefor |
US5543136A (en) | 1994-06-16 | 1996-08-06 | Nuskin International, Inc. | Sunscreen emulsions |
US5672337A (en) | 1994-12-12 | 1997-09-30 | L'oreal | Amido photostabilization of dibenzoylmethane sunscreens |
US5560917A (en) | 1995-02-01 | 1996-10-01 | Maybelline Intermediate Company | Cosmetic makeup composition |
US5770183A (en) | 1996-08-01 | 1998-06-23 | Linares; Francisco J. | High SPF (30 and over) waterproof sunblock compositions |
US6342208B1 (en) | 1996-08-02 | 2002-01-29 | Plum Kerni Produktion A/S | Oil-in-water emulsion containing C10-C24 fatty acid derivatives for treating skin of mammals |
US5824323A (en) | 1996-11-01 | 1998-10-20 | Absolute Beauty Company | Skin lotion composition and softgel filled therewith and methods for making and using same |
EP0848944A2 (en) | 1996-11-21 | 1998-06-24 | The C.P. Hall Company | Sunscreen composition comprising long, branched chain alkyl benzoates or hydroxybenzoates |
US6048517A (en) | 1996-11-25 | 2000-04-11 | Schering-Plough Healthcare Products, Inc. | High SPF sunscreen formulations |
US6159453A (en) | 1997-01-16 | 2000-12-12 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Sunscreens for protection from sun radiation |
US5863546A (en) | 1997-03-02 | 1999-01-26 | Swinehart; James M | Cosmetic composition |
US6007846A (en) | 1997-05-16 | 1999-12-28 | Townley Jewelry, Inc. | Scented body gel having particulate matter in the form of glitter with predetermined shapes |
US20020106337A1 (en) | 1997-05-27 | 2002-08-08 | Deckers Harm M. | Products for topical applications comprising oil bodies |
US6372234B1 (en) | 1997-05-27 | 2002-04-16 | Sembiosys Genetics Inc. | Products for topical applications comprising oil bodies |
US20020114820A1 (en) | 1997-05-27 | 2002-08-22 | Sembiosys Genetics Inc. | Products for topical applications comprising oil bodies |
US6162448A (en) | 1997-05-28 | 2000-12-19 | L'oreal | Combination of a retinoid with a polyamine polymer |
US6365630B1 (en) | 1997-06-04 | 2002-04-02 | Regents Of The University Of Michigan | Compositions and methods for inhibiting photoaging of skin |
US6090369A (en) | 1997-06-04 | 2000-07-18 | Stewart; Ernest Glading | Sunscreen formulation with avobenzone and method for stabilizing sunscreen formulation which contains avobenzone |
US6197281B1 (en) | 1997-06-04 | 2001-03-06 | Ernest G. Stewart | Wet appliable, instant protection sunscreen and makeup and method of use |
US6153208A (en) | 1997-09-12 | 2000-11-28 | The Procter & Gamble Company | Cleansing and conditioning article for skin or hair |
US6043204A (en) | 1997-11-07 | 2000-03-28 | Kaufman; Stacy R. | Body cleansing composition providing protection against sunburn after rinsing |
US6436374B1 (en) | 1997-11-12 | 2002-08-20 | Merck Patent Gesellschaft Mit Beschraenkter Haftung | Light-stable cosmetic formulation containing butylmethoxydibenzoylmethane |
US5985251A (en) | 1997-12-01 | 1999-11-16 | Roche Vitamins Inc. | Light screening compositions |
EP0930063A2 (en) | 1997-12-04 | 1999-07-21 | The C.P. Hall Company | Skin care and sunscreen composition |
US5976560A (en) | 1998-01-30 | 1999-11-02 | Han; Nam Fong | Vegetable derived petroleum jelly replacement |
US6355264B1 (en) | 1998-03-20 | 2002-03-12 | Avon Products, Inc. | Insect repellent composition |
US5961961A (en) | 1998-06-04 | 1999-10-05 | Chesebrough-Pond's Usa Co. | Sunscreen cosmetic composition |
US6521217B1 (en) | 1998-06-22 | 2003-02-18 | Ciba Specialty Chemicals Corporation | Sun screen formulations |
US20010026789A1 (en) | 1998-07-10 | 2001-10-04 | Herve Richard | Photostabilized sunscreen compositions comprising dibenzoylmethane compounds and benzylidenecamphor-substituted silanes/organosiloxanes |
US6290938B1 (en) | 1998-07-30 | 2001-09-18 | The Procter & Gamble Company | Sunscreen compositions |
US5989529A (en) | 1998-11-20 | 1999-11-23 | Schering-Plough Healthcare Products, Inc. | Substantive topical composition |
US6468509B2 (en) | 1998-12-18 | 2002-10-22 | Sol-Gel Technologies Ltd. | Sunscreen composition containing sol-gel microcapsules |
US20020037261A1 (en) | 1998-12-18 | 2002-03-28 | Nao Lapidot | Sunscreen composition containing sol-gel microcapsules |
US6071501A (en) | 1999-02-05 | 2000-06-06 | The Procter & Gamble Company | Photostable UV protection compositions |
US6165451A (en) | 1999-02-08 | 2000-12-26 | Roche Vitamins Inc. | Cosmetic light screening composition |
US20010014314A1 (en) | 1999-02-11 | 2001-08-16 | Marie Harbeck | Foot soap composition |
WO2000057850A1 (en) | 1999-03-25 | 2000-10-05 | Haarmann & Reimer | Photostable sunscreen compositions containing dibenzoylmethane derivative, e.g., parsol® 1789, and diesters or polyesters of naphthalene dicarboxylic acid photostabilizers and enhancers of the sun protection factor (spf) |
US6224852B1 (en) | 1999-04-23 | 2001-05-01 | Unilever Home & Personal Care Usa | Liquid sunscreen compositions which both deposit and lather well |
US6338838B1 (en) | 1999-05-12 | 2002-01-15 | Roche Vitamins Inc. | Photostable cosmetic light screening compositions |
US6238650B1 (en) | 1999-05-26 | 2001-05-29 | Sol-Gel Technologies Ltd. | Sunscreen composition containing sol-gel microcapsules |
US6384023B2 (en) | 1999-05-28 | 2002-05-07 | Neutrogena Corporation | Silicone gel containing salicylic acid |
US6322776B1 (en) | 1999-06-18 | 2001-11-27 | Schering-Plough Healthcare Products, Inc. | Anhydrous high-SPF ultraviolet light screens |
US6495122B2 (en) | 1999-07-12 | 2002-12-17 | Ciba Specialty Chemicals Corporation | Use of mixtures of micropigments for preventing tanning and for lightening skin and hair |
US6190645B1 (en) | 1999-07-15 | 2001-02-20 | Playtex Products, Inc. | Sunscreen for the scalp hair and hair |
US6395269B1 (en) | 1999-08-16 | 2002-05-28 | Playtex Products, Inc. | Sunscreen lotion or spray composition |
US6416748B1 (en) | 1999-10-22 | 2002-07-09 | Societe L'oreal | Emulsifier-free UV-photoprotecting emulsions comprising micronized insoluble screening agents |
US6352685B2 (en) | 1999-12-24 | 2002-03-05 | KOSé CORPORATION | External preparation for skin |
US20010031247A1 (en) | 2000-02-08 | 2001-10-18 | Martin Josso | UV-photoprotecting sunscreen compositions comprising immixture of polyethylene/carboxylated polyethylene polymers |
US6458372B1 (en) | 2000-03-08 | 2002-10-01 | Color Access, Inc. | Gel powder composition |
US6368639B1 (en) | 2000-03-24 | 2002-04-09 | Council Of Scientific And Industrial Research | Herbal skin care formulation and a process for the preparation thereof |
US6210658B1 (en) | 2000-06-12 | 2001-04-03 | The C. P. Hall Corporation | Stable sunscreen composition containing a barium compound, e.g., barium sulfate, a dibenzoylmethane derivative, e.g., butyl methoxydibenzoylmethane (avobenzone), and a methoxycinnamate derivative, e.g., octyl methoxycinnamate |
US20020012640A1 (en) | 2000-06-13 | 2002-01-31 | Fatemeh Mohammadi | Cosmetic composition for stressed skin under extreme conditions |
US20020028185A1 (en) | 2000-07-06 | 2002-03-07 | Fisher Gary J. | UVA (> 360-400) and UVB (300-325) specific sunscreens |
US20020028875A1 (en) | 2000-07-20 | 2002-03-07 | Anderle Gary A. | Plasticized waterborne polyurethane dispersions and manufacturing process |
US6458888B1 (en) | 2000-09-15 | 2002-10-01 | Isp Investments Inc. | Rheology modifier for use in aqueous compositions |
US6433061B1 (en) | 2000-10-24 | 2002-08-13 | Noveon Ip Holdings Corp. | Rheology modifying copolymer composition |
US6436376B1 (en) | 2001-02-26 | 2002-08-20 | Societe L'oreal S.A. | Enhanced SPF UV-sunscreen/tricontanyl PVP photoprotecting (sprayable) formulations |
US6436377B1 (en) | 2001-02-26 | 2002-08-20 | Societe L'oreal S.A. | Enhanced SPF sunscreen (sprayable) formulations comprising interpolymers of PVP/dimethiconylacrylate/polycarbamyl/polyglycol ester |
US6488915B1 (en) | 2001-03-15 | 2002-12-03 | Basf Aktiengesellschaft | Use of sunscreen combinations which comprise, as essential constituent, 2-(4-alkoxyanilinomethylene) malonic dialkyl esters as photostable UV filters in cosmetic and pharmaceutical preparations |
US6485712B1 (en) | 2001-05-24 | 2002-11-26 | Won Kyu Kim | UV blocking and slimming cosmetic composition |
US20020197217A1 (en) | 2001-06-06 | 2002-12-26 | Sewon Kang | Method and device for human skin tanning with reduced skin damage |
US6432389B1 (en) | 2001-07-06 | 2002-08-13 | Societe L'oreal | High SPF nontacky/nongreasy UV-photoprotecting compositions comprising particulates of MMA crosspolymers |
Non-Patent Citations (10)
Title |
---|
A New Thickener Stabilizer Technology; 1993, 108 (5), 61-67; Kopolow, Kwak, & Helioff. |
A New Thickener/Stabilizer Technology; Cosmetics & Toiletries, vol. 108, No. 5, May, p. 61-67, 1993; Kopolow, Kwak, & Helioff. |
Al-MG-Hydroxystearate: A New Rheological Additive and Stabilizer 1991, Cosmet Toiletries, 106 (8), 53-59. |
Al-Mg-hydroxystearate: New Rheological Additive and Stabilizer; Cosmetics & Toiletries, vol. 106 No: Aug. 1991, pp. 53-54, 56, 58-59; Giulini Chem. |
Cosmetic Lipogels Made From Aluminum-Magnesium-Hydroxy-Stearate, 1990 16<SUP>th </SUP>Congress of the IFSCC: Cosmetic Science in the 1990's and Beyond. |
European Search Report under Section 18 (3) dated Jun. 3, 2005. |
FUCOGEL 1000, The Significance of the Efficacy/smoothness Pair; 1996, pp. 265-274; J. Molina. |
Rheox-Waterborne Polysaccharide Thickener; Drug & Cosmetic Industry, No. Cosmetic Product News (Suppl.) Aug. 31, 1998, pp. 11. |
Secondary Structural Rheology of a Model Cream; J Soc Cosmet Chem, 1994 45 (2), 77-84; Pena, Lee, & Stearns. |
The NY Hilton, NYC, USA, Oct. 8-11, 1990, vol. 2, 456-467; U. Assmus. |
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Also Published As
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WO2003103615A1 (en) | 2003-12-18 | application |
CA2488335C (en) | 2011-05-24 | grant |
GB2407268B (en) | 2006-11-22 | grant |
GB2407268A (en) | 2005-04-27 | application |
US20040028709A1 (en) | 2004-02-12 | application |
GB0500022D0 (en) | 2005-02-09 | grant |
CA2488335A1 (en) | 2003-12-18 | application |
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